104578-89-4

Basic information

• Product Name: 2-Deoxy-L-ribose-anilide
• Synonyms: 2-Deoxy-L-ribose-anilide;2-Deoxy-N-phenyl-L-erythropentofuranosylamine;L-erythro-PentofuranosylaMine, 2-deoxy-N-phenyl-
• CAS NO: 104578-89-4
• Molecular Formula: C₁₁H₁₅NO₃
• Molecular Weight: 209.2417
• EINECS: 600-579-5
• Mol File: 104578-89-4.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 439.4±45.0 °C(Predicted)
• Appearance: /
• Density: 1.305
• Refractive Index: 1.631
• PKA: 13.81±0.60(Predicted)
• CAS DataBase Reference: 2-Deoxy-L-ribose-anilide(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Deoxy-L-ribose-anilide(104578-89-4)
• EPA Substance Registry System: 2-Deoxy-L-ribose-anilide(104578-89-4)

Safety Data

• Hazardous Substances Data: 104578-89-4(Hazardous Substances Data)

Usage

General Description

2-Deoxy-L-ribose-anilide is a chemical compound that is derived from the sugar 2-deoxyribose and aniline, an aromatic amine. It is a white powder that is soluble in organic solvents and has potential applications in pharmaceuticals and organic synthesis. 2-Deoxy-L-ribose-anilide has been studied for its potential use as a building block in the synthesis of nucleoside analogues, which are molecules that mimic the structure of natural nucleosides and have potential anti-cancer and antiviral properties. Additionally, 2-Deoxy-L-ribose-anilide may also have potential applications in the development of novel materials and as a reagent in chemical research and development. However, further research is needed to fully understand and utilize the potential of this compound.

InChI:InChI=1/C11H15NO3/c13-7-10-9(14)6-11(15-10)12-8-4-2-1-3-5-8/h1-5,9-14H,6-7H2/t9-,10+,11?/m1/s1

Upstream product

• 62-53-3 aniline 
• 38996-14-4 (4R,5S)-4-hydroxy-5-(hydroxymethyl)dihydrofuran-2(3H)-one 
• 104578-88-3 methyl (3R,4S)-3-(tert-butyldimethylsiloxy)-4,5-(isopropylidenedioxy)pentanoate 
• 364042-57-9 4-cyano-4-deoxy-1,2-O-isopropylidene-D-erythritol 
• 29780-54-9 (4R,5S)-5-(hydroxymethyl)tetrahydrofuran-2,4-diol 

Relevant articles and documents

A new efficient and practical synthesis of 2-deoxy-L-ribose

An efficient and practical route for large-scale synthesis of 2-deoxy-l-ribose starting from l-ascorbic acid was developed in eight steps without chromatographic purification for all intermediates. Additionally, (2S,3R)-3,4-epoxy-1,2-O-isopropylidenebutane-1,2-diol, a versatile intermediate in carbohydrate synthesis, was also prepared readily in excellent yield as a key intermediate.

THE CHEMISTRY OF O-SILYLATED KETENE ACETALS; DIASTEREOSELECTIVE ALDOL REACTION OF 2,3-O-ISOPROPYLIDENE-D (AND L)-GLYCERALDEHYDES LEADING TO 2-DEOXY-D (AND L)-RIBOSES

Diastereoselective carbon-carbon bond forming reaction of 2,3-O-isopropylidene-D (and L)-glyceraldehydes (D and L-2) with ketene silyl acetals (1a,b) occured in acetonitrile under mild conditions to give the corresponding anti-β-siloxyesters (D and L-3a) as major products, which could be converted through a few additional steps to 2-deoxy-D (and L)-riboses.